Antenatal corticosteroids and newborn screening for congenital adrenal hyperplasia

被引:13
作者
King, JL
Naber, JM
Hopkin, RJ
Repaske, DR
Bailey, L
Leslie, ND
机构
[1] Childrens Hosp Res Fdn, Div Human Genet, Cincinnati, OH 45229 USA
[2] Childrens Hosp Res Fdn, Div Endocrinol, Cincinnati, OH 45229 USA
[3] Univ Cincinnati, Coll Allied Hlth Sci, Genet Counseling Program, Cincinnati, OH USA
[4] Newborn Screening Program, Lansing, MI USA
来源
ARCHIVES OF PEDIATRICS & ADOLESCENT MEDICINE | 2001年 / 155卷 / 09期
关键词
D O I
10.1001/archpedi.155.9.1038
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objective: To assess the effect of reported corticosteroid exposure on neonatal levels of 17-hydroxyprogesterone (17-OHP), the cortisol precursor used in newborn screening for congenital adrenal hyperplasia, in newborns weighing less than 2500 g at birth. Design: A retrospective study of newborns weighing less than 2500 g at birth and exposed to corticosteroids as reported on their newborn screening card compared with newborns weighing less than 2500 g at birth and reported as not exposed to corticosteroids. Methods: Birth weight, gestational age, age at screening, special care information, and name of screening hospital were obtained from newborn screening cards for 16115 newborns screened in Michigan during the first 3 months of 2000. Levels of 17-OHP, measured by fluoroimmunoassay, were obtained from Michigan's Newborn Screening Program database. Results: The mean 17-OHP level for the 69 low-birthweight newborns in the corticosteroid-exposed group was 52 ng/mL, which was higher than that for the 771 low-birth-weight newborns in the unexposed group (35 ng/mL) (P<.001). Reported corticosteroid use did not decrease the number of expected borderline positive screening results for congenital adrenal hyperplasia (P>.05). Levels of 17-OHP varied by birth weight in corticosteroid-exposed and unexposed newborns. Conclusions: Corticosteroid exposure may not suppress screening 17-OHP levels. Therefore, newborn screening should not be delayed in premature newborns because of antenatal exposure to corticosteroids.
引用
收藏
页码:1038 / 1042
页数:5
相关论文
共 26 条
[11]   Methods to encourage the use of antenatal corticosteroid therapy for fetal maturation - A randomized controlled trial [J].
Leviton, LC ;
Goldenberg, RL ;
Baker, CS ;
Schwartz, RM ;
Freda, MC ;
Fish, LJ ;
Cliver, SP ;
Rouse, DJ ;
Chazotte, C ;
Merkatz, IR ;
Raczynski, JM .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1999, 281 (01) :46-52
[12]   MOLECULAR AND CLINICAL ADVANCES IN CONGENITAL ADRENAL-HYPERPLASIA [J].
MILLER, WL ;
LEVINE, LS .
JOURNAL OF PEDIATRICS, 1987, 111 (01) :1-17
[13]   Steroid disorders in children: Congenital adrenal hyperplasia and apparent mineralocorticoid excess [J].
New, MI ;
Wilson, RC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (22) :12790-12797
[14]  
*NEWB SCREEN COMM, 1999, NAT NEWB SCREEN REP
[15]   MICROFILTER PAPER METHOD FOR 17 ALPHA-HYDROXYPROGESTERONE RADIOIMMUNOASSAY - ITS APPLICATION FOR RAPID SCREENING FOR CONGENITAL ADRENAL-HYPERPLASIA [J].
PANG, S ;
HOTCHKISS, J ;
DRASH, AL ;
LEVINE, LS ;
NEW, MI .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1977, 45 (05) :1003-1008
[16]  
Pang S., 1993, SCREENING, V2, P105, DOI [10.1016/0925-6164(93)90024-D, 10.1016/0925-6164(93)90024-d]
[17]  
Pang Songya, 1997, Current Opinion in Pediatrics, V9, P419, DOI 10.1097/00008480-199708000-00018
[18]   Congenital adrenal hyperplasia [J].
Pang, SY .
ENDOCRINOLOGY AND METABOLISM CLINICS OF NORTH AMERICA, 1997, 26 (04) :853-+
[19]  
Spady DW, 1998, PEDIATRICS, V102, DOI 10.1542/peds.102.2.e21
[20]   MATERNAL GLUCOCORTICOID IN UNPLANNED PREMATURE LABOR - CONTROLLED-STUDY ON THE EFFECTS OF BETAMETHASONE PHOSPHATE ON THE PHOSPHOLIPIDS OF THE GASTRIC ASPIRATE AND ON THE ADRENAL-CORTICAL FUNCTION OF THE NEWBORN-INFANT [J].
TERAMO, K ;
HALLMAN, M ;
RAIVIO, KO .
PEDIATRIC RESEARCH, 1980, 14 (04) :326-329